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Ectodermal Wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton

The gill skeleton of cartilaginous fishes (sharks, skates, rays, and holocephalans) exhibits a striking anterior–posterior polarity, with a series of fine appendages called branchial rays projecting from the posterior margin of the gill arch cartilages. We previously demonstrated in the skate (Leuco...

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Autores principales: Rees, Jenaid M, Sleight, Victoria A, Clark, Stephen J, Nakamura, Tetsuya, Gillis, J Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027317/
https://www.ncbi.nlm.nih.gov/pubmed/36940244
http://dx.doi.org/10.7554/eLife.79964
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author Rees, Jenaid M
Sleight, Victoria A
Clark, Stephen J
Nakamura, Tetsuya
Gillis, J Andrew
author_facet Rees, Jenaid M
Sleight, Victoria A
Clark, Stephen J
Nakamura, Tetsuya
Gillis, J Andrew
author_sort Rees, Jenaid M
collection PubMed
description The gill skeleton of cartilaginous fishes (sharks, skates, rays, and holocephalans) exhibits a striking anterior–posterior polarity, with a series of fine appendages called branchial rays projecting from the posterior margin of the gill arch cartilages. We previously demonstrated in the skate (Leucoraja erinacea) that branchial rays derive from a posterior domain of pharyngeal arch mesenchyme that is responsive to Sonic hedgehog (Shh) signaling from a distal gill arch epithelial ridge (GAER) signaling centre. However, how branchial ray progenitors are specified exclusively within posterior gill arch mesenchyme is not known. Here, we show that genes encoding several Wnt ligands are expressed in the ectoderm immediately adjacent to the skate GAER, and that these Wnt signals are transduced largely in the anterior arch environment. Using pharmacological manipulation, we show that inhibition of Wnt signalling results in an anterior expansion of Shh signal transduction in developing skate gill arches, and in the formation of ectopic anterior branchial ray cartilages. Our findings demonstrate that ectodermal Wnt signalling contributes to gill arch skeletal polarity in skate by restricting Shh signal transduction and chondrogenesis to the posterior arch environment and highlights the importance of signalling interactions at embryonic tissue boundaries for cell fate determination in vertebrate pharyngeal arches.
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spelling pubmed-100273172023-03-21 Ectodermal Wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton Rees, Jenaid M Sleight, Victoria A Clark, Stephen J Nakamura, Tetsuya Gillis, J Andrew eLife Developmental Biology The gill skeleton of cartilaginous fishes (sharks, skates, rays, and holocephalans) exhibits a striking anterior–posterior polarity, with a series of fine appendages called branchial rays projecting from the posterior margin of the gill arch cartilages. We previously demonstrated in the skate (Leucoraja erinacea) that branchial rays derive from a posterior domain of pharyngeal arch mesenchyme that is responsive to Sonic hedgehog (Shh) signaling from a distal gill arch epithelial ridge (GAER) signaling centre. However, how branchial ray progenitors are specified exclusively within posterior gill arch mesenchyme is not known. Here, we show that genes encoding several Wnt ligands are expressed in the ectoderm immediately adjacent to the skate GAER, and that these Wnt signals are transduced largely in the anterior arch environment. Using pharmacological manipulation, we show that inhibition of Wnt signalling results in an anterior expansion of Shh signal transduction in developing skate gill arches, and in the formation of ectopic anterior branchial ray cartilages. Our findings demonstrate that ectodermal Wnt signalling contributes to gill arch skeletal polarity in skate by restricting Shh signal transduction and chondrogenesis to the posterior arch environment and highlights the importance of signalling interactions at embryonic tissue boundaries for cell fate determination in vertebrate pharyngeal arches. eLife Sciences Publications, Ltd 2023-03-20 /pmc/articles/PMC10027317/ /pubmed/36940244 http://dx.doi.org/10.7554/eLife.79964 Text en © 2023, Rees et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Rees, Jenaid M
Sleight, Victoria A
Clark, Stephen J
Nakamura, Tetsuya
Gillis, J Andrew
Ectodermal Wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton
title Ectodermal Wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton
title_full Ectodermal Wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton
title_fullStr Ectodermal Wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton
title_full_unstemmed Ectodermal Wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton
title_short Ectodermal Wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton
title_sort ectodermal wnt signaling, cell fate determination, and polarity of the skate gill arch skeleton
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027317/
https://www.ncbi.nlm.nih.gov/pubmed/36940244
http://dx.doi.org/10.7554/eLife.79964
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